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Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis

Host-derived glutathione (GSH) is an essential source of cysteine for the intracellular pathogen Francisella tularensis. In a comprehensive transposon insertion sequencing screen, we identified several F. tularensis genes that play central and previously unappreciated roles in the utilization of GSH...

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Autores principales: Ramsey, Kathryn M., Ledvina, Hannah E., Tresko, Tenayaann M., Wandzilak, Jamie M., Tower, Catherine A., Tallo, Thomas, Schramm, Caroline E., Peterson, S. Brook, Skerrett, Shawn J., Mougous, Joseph D., Dove, Simon L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340319/
https://www.ncbi.nlm.nih.gov/pubmed/32492066
http://dx.doi.org/10.1371/journal.ppat.1008566
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author Ramsey, Kathryn M.
Ledvina, Hannah E.
Tresko, Tenayaann M.
Wandzilak, Jamie M.
Tower, Catherine A.
Tallo, Thomas
Schramm, Caroline E.
Peterson, S. Brook
Skerrett, Shawn J.
Mougous, Joseph D.
Dove, Simon L.
author_facet Ramsey, Kathryn M.
Ledvina, Hannah E.
Tresko, Tenayaann M.
Wandzilak, Jamie M.
Tower, Catherine A.
Tallo, Thomas
Schramm, Caroline E.
Peterson, S. Brook
Skerrett, Shawn J.
Mougous, Joseph D.
Dove, Simon L.
author_sort Ramsey, Kathryn M.
collection PubMed
description Host-derived glutathione (GSH) is an essential source of cysteine for the intracellular pathogen Francisella tularensis. In a comprehensive transposon insertion sequencing screen, we identified several F. tularensis genes that play central and previously unappreciated roles in the utilization of GSH during the growth of the bacterium in macrophages. We show that one of these, a gene we named dptA, encodes a proton-dependent oligopeptide transporter that enables growth of the organism on the dipeptide Cys-Gly, a key breakdown product of GSH generated by the enzyme γ-glutamyltranspeptidase (GGT). Although GGT was thought to be the principal enzyme involved in GSH breakdown in F. tularensis, our screen identified a second enzyme, referred to as ChaC, that is also involved in the utilization of exogenous GSH. However, unlike GGT and DptA, we show that the importance of ChaC in supporting intramacrophage growth extends beyond cysteine acquisition. Taken together, our findings provide a compendium of F. tularensis genes required for intracellular growth and identify new players in the metabolism of GSH that could be attractive targets for therapeutic intervention.
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spelling pubmed-73403192020-07-17 Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis Ramsey, Kathryn M. Ledvina, Hannah E. Tresko, Tenayaann M. Wandzilak, Jamie M. Tower, Catherine A. Tallo, Thomas Schramm, Caroline E. Peterson, S. Brook Skerrett, Shawn J. Mougous, Joseph D. Dove, Simon L. PLoS Pathog Research Article Host-derived glutathione (GSH) is an essential source of cysteine for the intracellular pathogen Francisella tularensis. In a comprehensive transposon insertion sequencing screen, we identified several F. tularensis genes that play central and previously unappreciated roles in the utilization of GSH during the growth of the bacterium in macrophages. We show that one of these, a gene we named dptA, encodes a proton-dependent oligopeptide transporter that enables growth of the organism on the dipeptide Cys-Gly, a key breakdown product of GSH generated by the enzyme γ-glutamyltranspeptidase (GGT). Although GGT was thought to be the principal enzyme involved in GSH breakdown in F. tularensis, our screen identified a second enzyme, referred to as ChaC, that is also involved in the utilization of exogenous GSH. However, unlike GGT and DptA, we show that the importance of ChaC in supporting intramacrophage growth extends beyond cysteine acquisition. Taken together, our findings provide a compendium of F. tularensis genes required for intracellular growth and identify new players in the metabolism of GSH that could be attractive targets for therapeutic intervention. Public Library of Science 2020-06-03 /pmc/articles/PMC7340319/ /pubmed/32492066 http://dx.doi.org/10.1371/journal.ppat.1008566 Text en © 2020 Ramsey et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ramsey, Kathryn M.
Ledvina, Hannah E.
Tresko, Tenayaann M.
Wandzilak, Jamie M.
Tower, Catherine A.
Tallo, Thomas
Schramm, Caroline E.
Peterson, S. Brook
Skerrett, Shawn J.
Mougous, Joseph D.
Dove, Simon L.
Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis
title Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis
title_full Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis
title_fullStr Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis
title_full_unstemmed Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis
title_short Tn-Seq reveals hidden complexity in the utilization of host-derived glutathione in Francisella tularensis
title_sort tn-seq reveals hidden complexity in the utilization of host-derived glutathione in francisella tularensis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340319/
https://www.ncbi.nlm.nih.gov/pubmed/32492066
http://dx.doi.org/10.1371/journal.ppat.1008566
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